International safety notice
Safety Notice for Kodak DirectView DR 9500, Carestream Health
Germany / BfArM · DEU · Nov 30, 2009
Key facts
| Title | Safety Notice for Kodak DirectView DR 9500, Carestream Health |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Kodak DirectView DR 9500, Carestream Health |
| Manufacturer | Safety Notice for Kodak DirectView DR 9500, Carestream Health |
| Models | 1.B1.P5, 4.5.1, 1704567160 |
| Date | Nov 30, 2009 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1